Movement disorders in 2016: from genes to phenotypes

Paolo Calabresi; N. Tambasco

doi:10.1016/S1474-4422(16)30345-3

Movement disorders in 2016: from genes to phenotypes

Paolo Calabresi, N. Tambasco

University Hospital of Perugia

Risultato della ricerca: Contributo in rivista › Articolo

2 Citazioni (Scopus)

Abstract

N/A

Lingua originale	Inglese
pagine (da-a)	9-10
Numero di pagine	2
Rivista	LANCET NEUROLOGY
Volume	16
Numero di pubblicazione	1
DOI	https://doi.org/10.1016/S1474-4422(16)30345-3
Stato di pubblicazione	Pubblicato - 2017

All Science Journal Classification (ASJC) codes

Neurologia (clinica)

Keywords

Genetic Variation
Humans
Leucine-Rich Repeat Serine-Threonine Protein Kinase-2
Movement Disorders
Mutation
Phenotype

Accesso al documento

10.1016/S1474-4422(16)30345-3

Altri file e collegamenti

Cita questo

@article{42e3017a8fda4108a959da181e3d93b6,

title = "Movement disorders in 2016: from genes to phenotypes",

abstract = "N/A",

keywords = "Genetic Variation, Humans, Leucine-Rich Repeat Serine-Threonine Protein Kinase-2, Movement Disorders, Mutation, Phenotype, Genetic Variation, Humans, Leucine-Rich Repeat Serine-Threonine Protein Kinase-2, Movement Disorders, Mutation, Phenotype",

author = "Paolo Calabresi and N. Tambasco",

year = "2017",

doi = "10.1016/S1474-4422(16)30345-3",

language = "English",

volume = "16",

pages = "9--10",

journal = "LANCET NEUROLOGY",

issn = "1474-4422",

publisher = "Lancet Publishing Group",

number = "1",

}

TY - JOUR

T1 - Movement disorders in 2016: from genes to phenotypes

AU - Calabresi, Paolo

AU - Tambasco, N.

PY - 2017

Y1 - 2017

N2 - N/A

AB - N/A

KW - Genetic Variation

KW - Humans

KW - Leucine-Rich Repeat Serine-Threonine Protein Kinase-2

KW - Movement Disorders

KW - Mutation

KW - Phenotype

KW - Genetic Variation

KW - Humans

KW - Leucine-Rich Repeat Serine-Threonine Protein Kinase-2

KW - Movement Disorders

KW - Mutation

KW - Phenotype

UR - https://publicatt.unicatt.it/handle/10807/173360

UR - https://www.scopus.com/inward/citedby.uri?partnerID=HzOxMe3b&scp=85003839011&origin=inward

UR - https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85003839011&origin=inward

U2 - 10.1016/S1474-4422(16)30345-3

DO - 10.1016/S1474-4422(16)30345-3

M3 - Article

SN - 1474-4422

VL - 16

SP - 9

EP - 10

JO - LANCET NEUROLOGY

JF - LANCET NEUROLOGY

IS - 1

ER -

Movement disorders in 2016: from genes to phenotypes

Abstract

All Science Journal Classification (ASJC) codes

Keywords

Accesso al documento

Altri file e collegamenti

Fingerprint

Cita questo